WO2022109516A1 - Liquid precursor injection for thin film deposition - Google Patents
Liquid precursor injection for thin film deposition Download PDFInfo
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- WO2022109516A1 WO2022109516A1 PCT/US2021/072113 US2021072113W WO2022109516A1 WO 2022109516 A1 WO2022109516 A1 WO 2022109516A1 US 2021072113 W US2021072113 W US 2021072113W WO 2022109516 A1 WO2022109516 A1 WO 2022109516A1
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- WO
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- Prior art keywords
- liquid
- liquid precursor
- precursor
- injection unit
- pressure
- Prior art date
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- 239000012705 liquid precursor Substances 0.000 title claims abstract description 397
- 238000002347 injection Methods 0.000 title claims abstract description 164
- 239000007924 injection Substances 0.000 title claims abstract description 164
- 238000000427 thin-film deposition Methods 0.000 title claims abstract description 80
- 239000007788 liquid Substances 0.000 claims abstract description 187
- 239000002243 precursor Substances 0.000 claims abstract description 130
- 238000000034 method Methods 0.000 claims abstract description 86
- 230000008016 vaporization Effects 0.000 claims abstract description 71
- 238000009834 vaporization Methods 0.000 claims abstract description 61
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 41
- 239000010409 thin film Substances 0.000 claims abstract description 23
- 239000007789 gas Substances 0.000 claims description 96
- 239000012159 carrier gas Substances 0.000 claims description 88
- 238000002156 mixing Methods 0.000 claims description 54
- 239000000203 mixture Substances 0.000 claims description 27
- 238000004519 manufacturing process Methods 0.000 claims description 19
- 238000005137 deposition process Methods 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 12
- 238000000354 decomposition reaction Methods 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 10
- 230000001105 regulatory effect Effects 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 238000000151 deposition Methods 0.000 abstract description 21
- 238000005516 engineering process Methods 0.000 abstract description 8
- 239000004065 semiconductor Substances 0.000 abstract description 8
- 238000012545 processing Methods 0.000 abstract description 4
- 230000008021 deposition Effects 0.000 description 15
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- 238000000231 atomic layer deposition Methods 0.000 description 12
- 238000005229 chemical vapour deposition Methods 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 11
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- -1 etc.) Inorganic materials 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 229910052786 argon Inorganic materials 0.000 description 7
- 229910052734 helium Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 238000010926 purge Methods 0.000 description 7
- 238000007789 sealing Methods 0.000 description 7
- 230000001276 controlling effect Effects 0.000 description 6
- 238000001514 detection method Methods 0.000 description 6
- 239000001307 helium Substances 0.000 description 6
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 6
- 238000002716 delivery method Methods 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 101100408787 Arabidopsis thaliana PNSL1 gene Proteins 0.000 description 4
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- 230000003247 decreasing effect Effects 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000469 dry deposition Methods 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000004770 chalcogenides Chemical class 0.000 description 2
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- 230000000694 effects Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000007736 thin film deposition technique Methods 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 230000001052 transient effect Effects 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229910052691 Erbium Inorganic materials 0.000 description 1
- 229910000618 GeSbTe Inorganic materials 0.000 description 1
- 241000877463 Lanio Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910003098 YBa2Cu3O7−x Inorganic materials 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 238000001505 atmospheric-pressure chemical vapour deposition Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000009718 spray deposition Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000002887 superconductor Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/448—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials
- C23C16/4486—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials by producing an aerosol and subsequent evaporation of the droplets or particles
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45512—Premixing before introduction in the reaction chamber
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
- C23C16/45544—Atomic layer deposition [ALD] characterized by the apparatus
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45557—Pulsed pressure or control pressure
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/52—Controlling or regulating the coating process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/54—Apparatus specially adapted for continuous coating
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/3244—Gas supply means
- H01J37/32449—Gas control, e.g. control of the gas flow
Definitions
- the disclosed technology relates generally to semiconductor processing and more particularly to liquid precursor injection apparatus and methods for depositing thin films.
- Various thin films can be deposited using various techniques, including wet and dry deposition methods.
- Wet deposition methods include, e.g., aerosol/spray deposition, sol-gel method and spin-coating.
- Dry deposition methods include physical vapor-based techniques, e.g., physical vapor deposition (PVD) and evaporation. Dry deposition methods additionally include precursor and/or chemical reaction-based techniques, e.g., chemical vapor deposition (CVD) and atomic layer deposition (ALD).
- CVD chemical vapor deposition
- ALD atomic layer deposition
- a method of injecting a liquid precursor into a thin film deposition chamber comprises delivering a vaporized liquid precursor into the thin film deposition chamber by atomizing the liquid precursor into atomized precursor droplets using a liquid injection unit and vaporizing the atomized precursor droplets into the vaporized liquid precursor in a vaporization chamber.
- the liquid injector unit and the liquid precursor are such that operating the liquid precursor delivery unit under a lower stability condition, including a first liquid precursor temperature at the liquid injection unit, a first liquid precursor pressure upstream of the liquid precursor injection unit and a first gas pressure downstream of the liquid precursor injection unit, causes a mass flow rate of the liquid precursor to vary by more than 10% relative to an average mass flow rate of the liquid precursor during a first time duration.
- Delivering the vaporized liquid precursor into the thin film deposition chamber comprises operating the liquid precursor delivery unit under a higher stability condition.
- the higher stability includes one or more of: a second liquid precursor temperature at the liquid injection unit that is lower than the first liquid precursor temperature; a second liquid pressure upstream of the injection unit that is higher than the first liquid pressure; and a second gas pressure downstream of the liquid injection unit that is higher than the first Gas pressure.
- the higher stability is such that that the mass flow rate of the liquid precursor varies by less than 10% relative to an average mass flow rate during a second time duration having the same time duration as the first time duration.
- a method of delivering a liquid precursor into a thin film deposition chamber comprises providing a liquid precursor delivery unit configured to deliver a vaporized liquid precursor into the thin film deposition chamber by atomizing the liquid precursor into atomized precursor droplets using a liquid injection unit and vaporizing the atomized precursor droplets into the vaporized liquid precursor in a vaporization chamber.
- the method additionally includes delivering a vaporized liquid precursor into the thin film deposition chamber under a lower stability condition, which includes a first liquid precursor temperature at the liquid injection unit, a first liquid precursor pressure upstream of the liquid precursor injection unit and a first gas pressure downstream of the liquid precursor injection unit.
- the method additionally includes detecting a variation in mass flow rate of the liquid precursor that is greater than 10% relative to an average mass flow rate of the liquid precursor during a first time duration.
- the method further comprises delivering the vaporized liquid precursor into the thin film deposition chamber under a higher stability condition.
- the higher stability condition includes one or more of: a second liquid precursor temperature at the liquid injection unit that is lower than the first liquid precursor temperature; a second liquid precursor pressure upstream of the injection unit that is higher than the first liquid precursor pressure; and a second gas pressure downstream of the liquid injection unit that is higher than the first gas pressure.
- the higher stability condition is such that the mass flow rate of the liquid precursor varies by less than 10% relative to an average mass flow rate during a second time duration having the same time duration as the first time duration.
- an apparatus for delivering a liquid precursor into a thin film deposition chamber comprises a liquid precursor delivery system configured to deliver a vaporized liquid precursor into the thin film deposition chamber.
- the liquid precursor delivery system comprises a liquid injection unit configured to atomize the liquid precursor into atomized precursor droplets, a mixing area configured to receive the atomized precursor droplets from the liquid injection unit and to form a mixture including the atomized precursor droplets and a carrier gas, and a vaporization chamber configured to receive the mixture and to vaporize the atomized precursor droplets in the mixture to form the vaporized liquid precursor.
- the apparatus additionally comprises a liquid precursor delivery stability control system comprising one or more of: an injection unit temperature control system configured to sense and control a liquid precursor temperature at the liquid injection unit prior to being introduced into the mixing area; a carrier gas temperature control system configured to sense and control a carrier gas temperature prior to being introduced into the mixing area; a liquid push pressure control system configured to sense and control a liquid precursor pressure upstream of the liquid precursor injection unit; and a downstream gas pressure control system configured to sense and control a gas pressure downstream of the liquid precursor injection unit.
- a liquid precursor delivery stability control system comprising one or more of: an injection unit temperature control system configured to sense and control a liquid precursor temperature at the liquid injection unit prior to being introduced into the mixing area; a carrier gas temperature control system configured to sense and control a carrier gas temperature prior to being introduced into the mixing area; a liquid push pressure control system configured to sense and control a liquid precursor pressure upstream of the liquid precursor injection unit; and a downstream gas pressure control system configured to sense and control a gas pressure downstream of the liquid precursor injection unit.
- FIG. 1A illustrates a thin film deposition system configured to deliver a vaporized liquid precursor into a thin film deposition chamber, according to embodiments.
- FIG. IB illustrates the thin film deposition chamber of the thin film deposition system illustrated in FIG. 1A, according to embodiments.
- FIG. 2 illustrates a liquid precursor delivery unit for delivering a vaporized liquid precursor into a thin film deposition chamber, according to embodiments.
- FIGS. 3 A and 3B illustrate an example liquid precursor injection unit configured to atomize the liquid precursor into atomized precursor droplets, according to embodiments.
- FIG. 4 illustrates a method of delivering a liquid precursor into a thin film deposition chamber, according to embodiments.
- FIG. 5 illustrates a liquid precursor delivery stability control system for controlling the delivery of a vaporized liquid precursor into a thin film deposition chamber, according to embodiments.
- FIGS. 6A-6C illustrate thin film deposition processes in which the liquid precursor delivery methods and systems according to embodiments can be implemented.
- FIG. 7 illustrates an experimental graph of the mass flow rate as a function of time for a liquid precursor introduced into a thin film deposition chamber in pulse mode, using a liquid precursor delivery method according to embodiments.
- Cyclic deposition processes such as atomic layer deposition (ALD) processes can provide a relatively conformal conductive and insulating thin films on relatively high aspect-ratio (e.g., 2:1) structures with high uniformity. While generally less conformal and uniform compared to ALD, thin films deposited using continuous deposition processes such as chemical vapor deposition (CVD) can provide higher productivity and lower cost.
- ALD atomic layer deposition
- CVD chemical vapor deposition
- ALD and CVD can be used to deposit a variety of different films including elemental metals, semiconductors (e.g., Si, III-V, etc.), dielectrics (e.g., SiO2, AIN, HfO2, ZrO2, etc.), rare-earth oxides, conducting oxides and oxides (e.g., TiN, IrChetc.), ferroelectrics (e.g., PbTiOs, LaNiOs, etc.), superconductors (e.g., YBa2Cu3O7- x ), chalcogenides (e.g., GeSbTe), to name a few.
- elemental metals e.g., Si, III-V, etc.
- dielectrics e.g., SiO2, AIN, HfO2, ZrO2, etc.
- rare-earth oxides e.g., conducting oxides and oxides (e.g., TiN, IrChetc.)
- ferroelectrics
- precursors are delivered into a reactor and transported therein to a substrate, which may be heated, to deposit the thin films.
- gaseous precursors having high vapor pressures e.g., >0.1 Torr
- not all precursors are in gaseous form at atmospheric pressure and ambient temperature.
- Many precursors are available in liquid form.
- delivery of liquid precursors into a reactor chamber with precision is relatively more difficult to control, which in turn makes it more difficult to control the composition, nanostructure and consistency of the resulting thin films using liquid precursors, compared to gas precursors.
- a bubbler technology may be used.
- a liquid precursor is stored inside a bubbler, typically a stainless steel canister, and an inert carrier gas (e.g., Ar, He or N2) is introduced inside the liquid to bubble.
- an inert carrier gas e.g., Ar, He or N2
- the precursor vapor saturates the atmosphere in the bubbler and thus generated vapor is introduced onto the substrate surface.
- the delivery of reactants in these technologies depends on parameters including the temperature of the bubbler, the carrier gas flow rate, and the pressure over the surface of the liquid. While bubbler-based techniques may work satisfactorily with some liquid precursors, they may not be suitable for precursors having relatively low vapor pressure.
- the maximum temperature to which the bubbler may be heated to may be limited to the decomposition temperature of the precursor.
- many liquid precursors have a relatively low decomposition temperature.
- the bubbler-based techniques may not be practical for precursors having a relatively narrow temperature window, e.g., less than about 150 °C, 100 °C or 50 °C between the temperature at which the vapor pressure is high enough for practical (e.g., >0.1 Torr) use and the temperature at which the precursor decomposes.
- the bubblerbased techniques may be limited to techniques that employ precursors that are stable at relatively high temperature.
- direct liquid injection refers to techniques that use liquid precursor delivery units, e.g., injectors, to feed the deposition zone in reactants.
- the liquid precursor remains in liquid form up to the point of injection into a low pressure deposition chamber under vacuum.
- the DLI-based techniques enables precision regulation of the liquid mass flow rate, even for precursors that have a relatively narrow temperature window between the temperature at which the vapor pressure is high enough for practical use (e.g., >0.1 Torr) and the temperature at which the precursor decomposes.
- the temperature window of the precursors used by the methods and systems of liquid precursor delivery may be less than 150 °C, 100 °C, 50 °C, 25 °C, or a temperature window between any of these values.
- the liquid precursor goes through an evaporation chamber where it is vaporized, and in other cases, the precursors reach the surface of a heated substrate in a liquid state, e.g., in the form of atomized liquid precursor droplets, which are then vaporized prior to decomposition. If the precursor is still in liquid phase when it reaches the substrate, the deposition method may be referred to as spray or aerosol pyrolysis, depending on the generation method of the liquid droplets. Some spray/aerosol pyrolysis processes may be called atmospheric pressure CVD, as usually the evaporation takes place in proximity of the substrate heated to high temperatures.
- the advantages of DLI-based techniques include relatively low temperature of the liquid precursor, e.g., room temperature, which makes it possible to use precursors with low thermal stability and low vapor pressure.
- the inventors have recognized that some conventional liquid delivery systems and methods can suffer from mass flow rate instability of the liquid precursor. Without being bound to any theory, the inventors have discovered that one of the causes of the mass flow rate instability may be associated with, among other things, unintended or excessive vaporization of the liquid precursor at or near a conventional valve or injector, upstream of the point of injection, prior to being injected at the point of injection into a low pressure area, e.g., a vaporization chamber. When delivered by a conventional valve or an injector, the liquid precursor is intended to remain in liquid phase up to the point of injection. However, the inventors have discovered that unintended vaporization of the liquid precursor can occur in substantial amounts upstream of the point of injection.
- the unintended vaporization upstream of the point of injection may occur in part because the liquid precursor may be heated close to a vaporization temperature at the point of injection, and/or because the gas pressure downstream of the valve or the injector may be at a pressure that is substantially lower that the vaporization pressure during deposition.
- unintended vaporization of the liquid precursor can occur in substantial amounts upstream of the point of injection.
- the vaporization of the liquid precursor upstream of the point of injection may lead to pockets of gas or bubbles therein, which can in turn lead to instabilities in the mass flow rate of the liquid precursor for depositing thin films in the thin film deposition chamber.
- systems and methods disclosed herein enable the delivery of the liquid precursor into a thin film deposition chamber with enhanced stability and repeatability of the mass flow rate of the liquid precursor.
- FIG. 1A illustrates a thin film deposition system configured to deliver a vaporized liquid precursor into a thin film deposition chamber, according to embodiments.
- the thin film deposition system 100 includes a liquid precursor delivery unit 112 configured to receive one or more liquid precursors from a liquid precursor panel 108.
- the liquid precursor delivery unit 112 is further configured to receive a carrier gas, e.g., hydrogen or an inert gas such as Ar or N2, the flow of which is controlled by a mass flow controller 114a, through a carrier gas line 114.
- the liquid precursor delivery unit 112 is configured to output one or more vaporized liquid precursors into a thin film deposition chamber 104.
- the thin film deposition chamber 104 is configured to receive the vaporized liquid precursors through one or more liquid precursor inlet lines 118, and further configured to receive one or more gas precursors, e.g., oxidants such as O2 or NH3, the flow of which is controlled by a mass flow controller 120a, through one or more gas precursor inlet lines 120 from a gas panel 116.
- gas precursors e.g., oxidants such as O2 or NH3
- the liquid panel 108 includes one or more liquid precursor source units 110-1, 110-2,...,110-n, which in turn comprise respective ones of liquid tanks 110a-l, 110a- 2,..., HOa-n configured to hold respective liquid precursors.
- the liquid tanks 110a-l, 110a- 2,..., HOa-n are connected to respective ones of push gas lines 110b- 1, 110b-2,..., HOb-n, and to respective ones of liquid delivery lines 110c- 1, 110c-2,... , 1 lOc-n.
- Respective ones of liquid flow meters (LFMs) 110d-l, 110d-2,..., HOd-n are disposed in the flow paths of the liquid delivery lines 110c-l, 110c-2,..., HOc-n between the liquid tanks 110a-l, 110a-2,..., 1 lOa-n and the liquid precursor delivery unit 112.
- liquid precursors are depicted as being introduced into a common liquid precursor delivery unit 112.
- a plurality of liquid precursor delivery units 112 may be present, where each precursor injection unit 112 is dedicated to a respective liquid precursor.
- a single carrier gas line 114 is depicted as being connected to the liquid precursor delivery unit 112.
- configurations are not so limited, and there can be a plurality carrier gas lines 114, where each carrier gas line is connected to a dedicated liquid injection unit 112, such that each liquid injection unit 112 received a dedicated liquid precursor and a dedicated carrier gas (e.g., FIG. 2).
- Each of the liquid precursor source units 110-1, 110-2,..., 110-n may be qualitatively operated in a similar manner.
- a push gas e.g., hydrogen or an inert gas such as helium, argon or nitrogen
- a gas mass flow controller not shown
- the push gas pushes the liquid precursor out of the liquid tank 110a-l
- the liquid delivery line 110c-l delivers the liquid precursor pushed out from the liquid tank 110a- 1 to the liquid precursor delivery unit 112.
- FIG. IB illustrates a thin film deposition chamber of a thin film deposition system, e.g., the thin film deposition system 100 described above with respect to FIG. 1A, according to embodiments.
- the thin film deposition chamber 104 includes a chamber housing 111 configured to seal the chamber airtight under a vacuum.
- the lower portion of the thin film deposition chamber 104 includes a susceptor 124 having a top surface 124S configured for a substrate 117 to be disposed thereon.
- the susceptor 124 can be heated to a process temperature by a heater 115.
- the susceptor 124 may be rotated about an axis of rotation D to improve film uniformity. The rotation can take place relative to a central axis.
- a vacuum pump (not shown) connected to the thin film deposition chamber 104 via an outlet 128 is configured to evacuate gases in the thin film deposition chamber 104.
- the upper portion of the thin film deposition chamber 104 includes a gas distribution plate or a showerhead 113 having a plurality of openings to eject a mixture of gases therethrough over the substrate 117.
- One or more liquid precursor inlet lines 118 configured to deliver vaporized liquid precursors from the liquid precursor delivery unit 112 and one or more gas precursor inlet lines 120 configured to deliver respective gas precursors, e.g., oxidants from the gas panel 116, are connected to the showerhead 113.
- One or more mass flow meters 132 may be disposed in the paths of the liquid precursor inlet lines 118 and gas precursor inlet lines 120 to measure the mass flow rate of the vaporized liquid precursor and the gas precursors.
- the variation in a mass flow rate of the vaporized liquid precursor(s) may be sensed by a liquid precursor delivery stability control system 500 (FIG.5), to activate a method of delivering the liquid precursor at a higher stability condition, according to various embodiments disclosed herein.
- the liquid precursor delivery stability control system 500 may trigger a method 400 (FIG. 4) according to embodiments.
- FIG. 2 illustrates a liquid precursor injection system for delivering a vaporized liquid precursor into a thin film deposition chamber, e.g., the thin film deposition chamber described above with respect to FIG. IB, according to embodiments.
- the liquid precursor injection system 200 includes a liquid precursor delivery unit 112.
- the liquid precursor delivery unit 112 includes a liquid injection unit 204 configured to receive a liquid precursor in liquid phase from a liquid precursor source unit 110.
- the liquid precursor source unit 110 includes a liquid tank 110a having stored therein a liquid precursor 228.
- a push gas line 110b is connected to the liquid tank 110a through a pressure regulator 224.
- the liquid delivery line 110c is connected to the liquid injection unit 204 configured to atomize the liquid precursor 228.
- Atomization refers to a process in which the liquid precursor is formed into a spray of liquid precursor droplets.
- Atomized liquid droplets can have, e.g., an average diameter of about 1 pm -100 pm.
- the droplets have a ratio of high surface area to volume, and are optimized for rapid evaporation into a vaporized liquid precursor.
- a push gas e.g., hydrogen or an inert gas such as helium, argon or nitrogen is supplied through the push gas line 110b to the liquid tank 110a, in order to displace the liquid precursor 228 from the liquid tank 110a.
- the gas stream flowing through the push gas line 110b can be regulated by the pressure regulator 224.
- displaced liquid precursor is delivered to the liquid injection unit 204 through the liquid delivery line 110c.
- the liquid precursor delivery unit 112 additionally includes a carrier gas valve 208 configured to receive a carrier gas, which may be hydrogen or an inert gas such as helium, argon or nitrogen, through a carrier gas line 114.
- a carrier gas heater 220 may be disposed in the path of the carrier gas line 114 to regulate the temperature of the carrier gas delivered to the carrier gas valve 208.
- the liquid precursor delivery unit 112 additionally includes a mixing area 212 downstream of the liquid injection unit 204 and the carrier gas valve 208 and configured to mix the atomized liquid precursor droplets and the carrier gas to form an atomized liquid precursor mixture.
- the liquid injection unit 204 and the carrier gas valve 208 are configured to inject the atomized precursor droplets and the carrier gas, respectively, into the mixing area 212.
- the trajectory of the atomized precursor droplets ejected from the liquid injection unit 204 and the trajectory of the carrier gas ejected from the carrier gas valve 208 may cross at a mixing point within the mixing area 212, such that the atomized liquid precursor mixture is efficiently formed by the mixing of the atomized precursor droplets and the carrier gas, prior to being vaporized.
- the atomized liquid precursor mixture formed from the atomized precursor droplets and the carrier gas formed in the mixing area 212 is subsequently introduced into a vaporization chamber 216.
- the vaporization chamber 216 is configured to vaporize the atomized precursor droplets in the atomized liquid precursor mixture to form a vaporized liquid precursor mixture including the vaporized liquid precursor and the carrier gas.
- the vaporization chamber 216 can have a volume of approximately one to three liters.
- the vaporization chamber 216 comprises vaporization means, e.g., a healer. Tor example, the vaporization of the atomized precursor droplets may be achieved in part by heated the walls of the vaporization chamber 216.
- the walls of the vaporization chamber 216 may be heated, e.g., to a temperature such that the atomized precursor droplets are heated to a temperature between the vaporization temperature and the decomposition temperature of the liquid precursor at atmospheric pressure.
- a temperature between the vaporization temperature and the decomposition temperature of the liquid precursor at atmospheric pressure For example, for a liquid precursor having a vaporization temperature of 200 °C and a decomposition temperature of 250 °C at atmospheric pressure, the vaporization chamber 216 may be heated to a temperature between 200 °C and 250 °C.
- the vaporization chamber 216 is configured to deliver the thus formed vaporized liquid precursor mixture into the thin film deposition chamber 104 through liquid precursor inlet 118 and further through a shower head 113, as described above with respect to FIGS. 1A and IB.
- One or more gas precursors, e.g., oxidants from the gas panel 116 are delivered through gas precursor inlets 120 also connected to the shower head 113, as described above with respect to
- the mixing area 212 and the vaporization chamber 216 may be configured to be at a local pressure that is higher than the deposition chamber pressure.
- the higher local pressure may be achieved by designing the shapes of internal volumes of the mixing area 212 and/or the vaporization chamber 216 to limit their conductance.
- one or both of the mixing area 212 and the vaporization chamber 216 may include an elongated section that is elongated in a vertical direction perpendicular to the plane of the showerhead 113, such that a pressure gradient exists in the vertical direction.
- one or both of the mixing area 212 and/or the vaporization chamber 216 may have an aspect ratio between a length in the vertical direction and a width or diameter in a horizontal direction that is greater than 2:1, 4:1, 6:1, 8:1, 10:1 or a value in a range defined by any of these values.
- the mixing area 212 and/or the vaporization chamber 216 may be partially hindered for evacuation, e.g., by a conductance-limiting orifice.
- one or both of the mixing area 212 the vaporization chamber 216 may include a continuously adjustable conductancecontrolling means at lower portions thereof, e.g., a pressure regulator or a butterfly valve and the like, such that the local pressures therein are higher than that of the deposition chamber pressure.
- the conductance-controlling means can be disposed between the mixing area 212 and the vaporization chamber 216, and/or between the vaporization chamber 216 and the thin film deposition chamber 104, e.g., upstream of the showerhead 113.
- the mixing area 212 and the vaporization chamber 216 are depicted as separate chambers. However, configurations are not so limited, and in other configurations, the mixing area 212 may form a portion of the vaporization chamber 216 while having different shape and size of the internal volume, e.g., an elongated volume as described above. In yet some other configurations, the mixing area 212 may be omitted, and the atomized liquid precursor and the carrier gas may be directly introduced into the vaporization chamber 216.
- the liquid injection unit 204 can include a suitable means configured to atomize the liquid precursor into atomized precursor droplets or aerosol.
- the liquid injection unit 204 can include a metering valve.
- FIGS. 3 A and 3B illustrate an example liquid precursor injection unit 204 comprising a metering valve 304 configured to atomize the liquid precursor into atomized precursor droplets, according to embodiments.
- the depicted example of the metering valve 304 is similar to a PICOTM valve manufactured by Nordson EFD LLC, the specification and design of which is incorporated herein by reference in its entirety.
- FIG. 3A depicts the metering valve 304 in a closed state and FIG.
- the metering valve 304 includes an inlet 302 connected to the liquid delivery line 110c for receiving the liquid precursor 228 from the liquid precursor source unit 110 (FIG. 2), and an outlet 320 connected to the mixing area 212 (FIG. 2).
- the metering valve 304 includes a lever 308 configured to be driven by piezoelectric actuators to move up and down as indicated by the arrows.
- the lever 308 has a distal end at which a vertical rod 312 is movably connected thereto. The movement of the lever 308 causes a corresponding vertical movement of the rod 312, as indicated by the arrows.
- a hemispherical sealing ball 316 formed of a wear-resistant ceramic is disposed at a bottom end of the rod 312.
- a ceramic valve seat 318 also referred to as a nozzle plate, is disposed below the sealing ball 316.
- the ceramic valve seat 318 has an opening that is smaller than a diameter of the sealing ball 316.
- the opening can have a diameter of, e.g., 50 pm to 500 pm.
- the opening of the valve seat 318 may represent a point of injection. As described herein, the point of injection defines a region within a liquid injection unit 204 at which the liquid precursor 228 is atomized into atomized precursor droplets.
- the point of injection also defines a point which divides an upstream portion of the metering valve 304 in which the liquid precursor is in liquid state, and a downstream portion of the metering valve 304 which is exposed to a low pressure region, e.g., the mixing area 212.
- the injection unit 204 can include a mass flow meter, which does not include a controllable valve, where varying the driving pressure exerted on it results in varying liquid flow rate.
- FIG. 4 illustrates a method of delivering a liquid precursor into a thin film deposition chamber, according to embodiments.
- FIG. 5 illustrates a liquid precursor delivery stability control system for controlling the delivery of a vaporized liquid precursor into a thin film deposition chamber, according to embodiments.
- the method 400 (FIG. 4) of delivering the liquid precursor is described in conjunction with the control system 500 (FIG. 5).
- the liquid precursor delivery control system 500 for controlling the delivery of a vaporized liquid precursor into a thin film deposition chamber includes a liquid push pressure control system 510, an injection unit temperature control system 520, a carrier gas temperature control system 530 and a downstream pressure control system 540 that are communicatively coupled to each other, and are communicatively coupled to a central control unit 550.
- the liquid push pressure control system 510 which may be disposed upstream of the liquid injection unit 204 (FIG. 2) is configured to control the liquid precursor push pressure in the liquid delivery line 110c (FIG. 2) upstream of the liquid precursor injection unit 112 (FIG.
- the injection unit temperature control system 520 which may be disposed at or upstream of the liquid injection unit 204 (FIG. 2), is configured to control the liquid precursor temperature at or above the liquid injection unit 204 (FIG. 2), using a liquid temperature sensing means 524 and a liquid temperature control means 528 that are communicatively coupled to each other.
- the carrier gas temperature control system 530 which may be disposed at or upstream of the carrier gas valve 208 (FIG. 2), is configured to control the carrier gas temperature at or above the carrier gas valve 208 (FIG.
- the downstream pressure control system 540 which may be disposed downstream of the liquid injection unit 204 (FIG. 2), is configured to control the gas pressure downstream of the liquid injection unit 204 (FIG. 2), using a gas pressure sensing means 544 and a gas pressure control means 548 that are communicatively coupled to each other.
- Each of the liquid pressure sensing means 514 and the gas pressure sensing means 544 can include a suitable pressure sensor, e.g., a manometer, a transducer and the like.
- Each of the liquid temperature sensing means 524 and the carrier gas temperature sensing means 534 can include a suitable temperature sensor, e.g., thermocouple, thermistor, resistance temperature detector and the like.
- Each of the liquid pressure control means 518 and the gas pressure control means 548 can include a pressure regulator, a control valve and the like, which can be controlled by a suitable controller circuitry and/or algorithm.
- Each of the liquid temperature control means 528 and the carrier gas temperature control means 538 can include a heater and/or cooler, which can be controlled by an internal or external controller circuitry and/or algorithm.
- each of the liquid push pressure control system 510, the injection unit temperature control system 520, the carrier gas temperature control system 530 and the downstream pressure control system 540, as well as the respective sensing means and the control means included therein are communicatively coupled to each other and to the central control or processing unit 550.
- the central control or processing unit 550 includes a processor, memory and storage devices that are collectively configured to store and execute executable algorithm for communicating with and at least partly automatically controlling the liquid push pressure control system 510, the injection unit temperature control system 520, the carrier gas temperature control system 530 and the downstream pressure control system 540, thereby implementing part or all of the method 400 automatically or algorithmically.
- one or more of the liquid push pressure control system 510, the injection unit temperature control system 520, the carrier gas temperature control system 530 and the downstream pressure control system 540 may be activated upon detection of a mass flow rate variation that is out of range of a predefined manufacturing tolerance.
- the flow rate variation may be detected by, e.g., the mass flow meters 132 (FIG. IB).
- one or more of the liquid pressure control means 518, the liquid temperature control means 528, the carrier gas temperature control means 538 and the gas pressure control means 548 may at least partly automatically or algorithmically regulate the liquid push pressure in the liquid delivery line 110c (FIG. 2), the liquid precursor temperature at or above the liquid injection unit 204 (FIG. 2), the carrier gas temperature at or above the carrier gas valve 208 (FIG. 2) and the gas pressure downstream of the liquid injection unit 204 (FIG. 2), respectively, in conjunction with the central control unit 550.
- the method 400 of delivering a liquid precursor into a thin film deposition chamber includes providing 410 a liquid precursor delivery unit 112 (FIG. 2) configured to deliver a vaporized liquid precursor 228 (FIG. 2) into the thin film deposition chamber 104 (FIG. 2).
- the liquid precursor delivery unit 112 comprises a liquid injection unit 204 (FIG. 2) configured to atomize the liquid precursor into atomized precursor droplets and a vaporization chamber 216 (FIG. 2) configured to vaporize the atomized precursor droplets prior to delivery into the thin film deposition chamber 104 (FIG. 2).
- the method additionally includes delivering the vaporized liquid precursor into the thin film deposition chamber 104 using the liquid precursor delivery unit 112, wherein delivering the vaporized liquid precursor comprises atomizing the liquid precursor 228 into atomized precursor droplets using the liquid injection unit 204 and vaporizing the atomized precursor droplets into the vaporized liquid precursor using the vaporization chamber 216.
- the liquid precursor delivery unit 112 and the liquid precursor 228 are such that, when the liquid precursor delivery unit 112 is operated under a lower stability condition, a mass flow rate of the liquid precursor varies by more than a manufacturing tolerance relative to an average mass flow rate of the liquid precursor 228 during a first time duration.
- the lower stability condition that causes such variation includes one or more of a first liquid precursor temperature (TPLI) at the liquid injection unit 204 (FIG. 2), a first liquid precursor pressure (PPLI) upstream of the liquid injection unit 204 and a first gas pressure (PPGI) downstream of the liquid injection unit 204.
- TPLI first liquid precursor temperature
- PPLI first liquid precursor pressure
- PPGI first gas pressure downstream of the liquid injection unit 204.
- the inventors have discovered that such variation in the mass flow rate can lead to manufacturing nonuniformities, including variations in thickness, composition and film quality such as density across the substrate as well as across different substrates.
- the inventors have discovered that operating 420 the liquid precursor delivery unit 112 under a higher stability condition causes the mass flow rate of the liquid precursor vary by less than the manufacturing tolerance relative to an average mass flow rate during a second time duration having the same time duration as the first time duration.
- operating 420 the liquid precursor delivery unit 112 under the higher stability condition includes one or more of: setting or decreasing 424 the temperature of the liquid precursor 228 to a second liquid precursor temperature (TPL2) at the liquid injection unit 204 (FIG. 2) that is lower than the first liquid precursor temperature (TPLI); setting or increasing 426 the pressure of the liquid precursor 228 to a second liquid precursor pressure (PPL2) upstream of the injection unit that is higher than the first liquid precursor pressure (PPLI); and setting or increasing 428 the gas pressure downstream of the liquid injection unit 204 to a second gas pressure (PPG2) downstream of the liquid injection unit 204 that is higher than the first downstream pressure (PPGI).
- TPL2 second liquid precursor temperature
- PPL2 second liquid precursor pressure
- PPG2 second gas pressure
- the inventors have discovered that operating 420 the liquid precursor delivery unit 112 (FIG. 2) under the higher stability condition according to various embodiments disclosed herein advantageously enables the delivery of the liquid precursor 228 into the thin film deposition chamber 104 (FIG. 2) with enhanced stability and repeatability.
- the enhanced stability and repeatability is enabled at least in part by, among other things, keeping the liquid precursor to remain in liquid phase and preventing vaporization of the liquid precursor upstream of the point of injection, as described above.
- the method 400 enables substantial suppression of the vaporization of the liquid precursor upstream of the point of injection, which in turn enables the suppression of formation of pockets of gas or bubbles being, thereby enabling enhanced stability of the vaporized precursor for depositing thin films in the thin film deposition chamber 104 (FIG. 2).
- a vaporization temperature refers to a temperature at which the vapor pressure of the liquid precursor is sufficient for deposition, e.g., the temperature at which the vapor pressure is greater than about 0.1 Torr, 0.2 Torr, 0.5 Torr, 1 Torr, or a value in a range defined by any of these values.
- the temperature of the liquid precursor 228 may be defined by proximity to the vaporization temperature and/or the decomposition temperature.
- the liquid precursor 228 (FIG. 2) at the liquid precursor delivery unit 112 (FIG. 2) or the point of injection therein may be within +/- 50°C, +/- 30°C, +/- 20°C, +/-10°C, or a value in a range defined by any of these values, of the vaporization temperature of the liquid precursor 228, or within 50°C, 30°C, 20°C, 10°C, or a value in a range defined by any of these values, below the decomposition temperature of the liquid precursor.
- the pressure downstream of the point of injection e.g., in the mixing area 212 (FIG. 2), the vaporization chamber 216 (FIG. 2) and/or the thin film deposition chamber 104 (FIG.
- the enhanced stability and repeatability may be quantified by the variability of the mass flow rate, which may be measured ty a mass flow meter 132 (FIG. IB) relative to a manufacturing tolerance.
- operating 420 the liquid precursor delivery unit 112 within a higher stability condition enables the mass flow rate of the liquid precursor to be maintained within a manufacturing tolerance.
- the manufacturing tolerance of the mass flow rate of the liquid precursor can be dependent on the application.
- the manufacturing tolerance may dictate that the mass flow rate not vary by not more than 1%, 2%, 5%, 10%, 20% or a value in a range defined by any of these values, relative to an average mass flow rate of the liquid precursor during a time duration longer than 1 ms, 5 ms, 10 ms, 20 ms, 50 ms, 100 ms, 200 ms, 500 ms, 1 sec, 2 sec, 5 sec, 10 sec, 20 sec, 50 sec, 100 sec, 200 sec, 500 sec, 1000 sec, 2000 sec, 5000 sec, 10,000 sec, 100,000 sec, 1,000,000 sec, or a time duration in a range defined by any of these values.
- the time duration may correspond to an aggregated exposure time of hundreds or thousands of wafer processes between successive preventive maintenance operations of the thin film deposition system.
- the time duration can represent an uninterrupted duration.
- the time duration can be the duration of a single pulse, or an aggregate sum of a plurality of depositions.
- the time duration can exclude transient effects such an initial spike or dip when the liquid precursor delivery unit 112 (FIG. 2) is initially activated.
- operating 420 the liquid precursor delivery unit 112 (FIG. 2) under the higher stability condition includes setting or decreasing 424 the temperature (TPL) of the liquid precursor 228 to a second liquid precursor temperature (TPL2) at the liquid injection unit 204 that is lower than the first liquid precursor temperature (TPLI) under the low stability condition.
- the TPL2 can in part be achieved by decreasing 424 the temperature of the liquid precursor 228 (FIG. 2) to the TPL2 at the liquid injection 112 (FIG. 2) using the injection unit temperature control system 520 (FIG. 5), or using the injection unit temperature control system 520 in conjunction with the carrier gas temperature control system 530 (FIG. 5).
- the injection unit temperature control system 520 is configured to actively control the temperature of the liquid precursor prior to being atomized into the mixing area 212 using the liquid temperature sensing means 524 and the liquid temperature control means 528.
- the liquid temperature sensing means 534 and the liquid temperature control means 528 may at least partly automatically or algorithmically regulate the liquid precursor temperature at or above the point of injection within the liquid injection unit 204 (FIG. 2) in conjunction with the central control unit 550.
- the liquid temperature control means 528 may include an active cooling means for lowering the (TPL) temperature of the liquid precursor 228 at the injection unit 204 (FIG. 2) prior to being atomized into the mixing area 212 (FIG. 2).
- first and the second liquid precursor temperatures (TPLI, TPL2) of the liquid precursor upstream e.g., immediately upstream, of the point of injection, may be set to or decreased to be within +/- 50 °C, +/- 30 °C, +/- 20 °C, +/-10 °C, or a value in a range defined by any of these values, of the vaporization temperature of the liquid precursor 228 at atmospheric pressure, or within 50°C, 30°C, 20°C, 10°C, or a value in a range defined by any of these values, below the decomposition temperature at atmospheric pressure of the liquid precursor 228 (FIG.
- the temperature of the liquid precursor may advantageously be set or lowered from the TPLI to TPL2 by at least 5 °C-50 °C, 5 °C- 10 °C, 10 °C-20 °C, 20 °C-30 °C, 40 °C-50 °C, or a value in a range defined by any of these values. It will be appreciated that the controlling the TPL within these range can be critical because, as discussed above, a TPL that is lower than these ranges can lead to inadequate vaporization of the liquid precursor, while a TPL that is higher than these ranges can lead to decomposition of the liquid precursor.
- the lowered second liquid precursor temperature (TPL2) of the liquid precursor 228 may at least partly compensated by heating carrier gas and mixing the atomized precursor droplets formed from the cooled liquid precursor with the heated carrier gas in the mixing are 212 (FIG. 2), as described below.
- the carrier gas temperature control system 530 is configured to actively control the temperature (TCG) of the carrier gas prior to being introduced into the mixing area 212 using the carrier gas temperature sensing means 534 and the carrier gas temperature control means 538.
- TCG temperature of the carrier gas
- the carrier gas temperature sensing means 534 and the carrier gas temperature control means 538 may at least partly automatically or algorithmically regulate the carrier gas temperature to be heated to and/or maintained at a higher temperature at the carrier gas valve 208 above the mixing area 212 (FIG. 2) in conjunction with the central control unit 550.
- the carrier gas valve 208 may be configured to actively control the temperature of the carrier gas prior be being delivered into the mixing area 212.
- the carrier gas temperature control system 530 may include an active heating means installed at the carrier gas valve 208.
- the carrier gas temperature control system 520 may include, e.g., the carrier gas temperature sensing means 534 configured to sense the temperature of the carrier gas upstream of the carrier gas valve 208 and, and a carrier gas temperature control means 538 including a heater to actively increase the temperature of the carrier gas prior to being introduced into the mixing area 212.
- the temperature of the carrier gas may be heated from a lower carrier temperature (TCGI) under the lower stability condition by at least 5 °C-50 °C, 5 °C- 10 °C, 10 °C-20 °C, 20 °C-30 °C, 40 °C-50 °C, or a value in a range defined by any of these values, to a higher carrier temperature (TCG2).
- TCGI lower carrier temperature
- heating the carrier gas to the TCG2 under the higher stability condition from the TCGI under the lower stability condition at least partly compensates the cooling effect of the liquid precursor as the liquid precursor is atomized into the mixing area 212 (FIG. 2).
- the temperature of the atomized liquid precursor mixture formed by the mixing the atomized precursor droplets formed from the liquid precursor at the second liquid precursor temperature (TPL2) with the heated carrier gas at the TCG2 can be, substantially the same as the temperature of the atomized liquid precursor mixture formed by mixing the atomized precursor droplets formed from the liquid precursor at the first liquid precursor temperature (TPLI) of the lower stability condition with the carrier gas at the TCGI prior to heating.
- the temperature change of the atomized liquid precursor mixture in the mixing area 212 between the lower an higher stability conditions may be within 5 °C-50 °C, 5 °C- 10 °C, 10 °C-20 °C, 20 °C-30 °C, 40 °C-50 °C, or a value in a range defined by any of these values. It will be appreciated that the controlling the temperature of the atomized precursor mixture within these range can be critical because lower temperatures can lead to inadequate vaporization of the liquid precursor, higher temperatures can lead to decomposition of the liquid precursor.
- operating 420 the liquid precursor delivery unit 112 (FIG. 2) under the higher stability condition includes setting or increasing 426 the liquid pressure (PPL) of the liquid precursor 228 to a second liquid pressure (PPL2) of the higher stability condition upstream of the point of injection in the injection unit 112 that is higher than the first liquid pressure (PPLI) of the lower stability condition upstream of the point of injection in the liquid injection unit 112.
- Setting or increasing 426 the liquid pressure of the liquid precursor 228 may be achieved using the liquid push pressure control system 510.
- the pressure of the push gas e.g., hydrogen or an inert gas such as helium, argon or nitrogen that is supplied through the push gas line 110b (FIG.
- the liquid push pressure control system 510 is configured to actively control the PPL of the liquid precursor 228 (FIG. 2) prior to being atomized into the mixing area 212 (FIG. 2) using the liquid pressure sensing means 514 and the liquid pressure control means 518.
- the liquid pressure sensing means 514 and the liquid pressure control means 518 may at least partly automatically or algorithmically regulate the liquid precursor pressure upstream of the liquid injection unit 204 (FIG. 2), e.g., at the liquid precursor source unit 110, in conjunction with the central control unit 550.
- setting or increasing the PPL upstream of the liquid injection unit 112 comprises regulating a liquid push gas at the liquid precursor source unit 110 (FIG. 2).
- the pressure regulator 224 is configured such that the liquid push pressure in the liquid delivery line 110c can be controlled to be within 10-50 psia, 10-15 psia, 15-20 psia, 20-25 psia, 25-30 psia, 30-35 psia, 35-40 psia, 40-45 psia, 45-50 psia, or a pressure in a range defined by any of these vales, for instance between 14 psia and 30 psia, e.g., 28 psia.
- operating 420 the liquid precursor delivery unit 112 under the higher stability condition includes setting or increasing 428 the gas pressure (PPG) downstream of the injection unit 112 to a second gas pressure (PPG2) that is higher than the first gas pressure (PPGI).
- PPG2 can be achieved at least in part by limiting the conductance in an area between the liquid injection unit 112 and the thin film deposition chamber 104 using the downstream pressure control system 540.
- increasing the PPG may be achieved by limiting the conductance to locally increase the PPG in one or both of the mixing area 212 and the vaporization chamber 216.
- the local increase in the PPG may be achieved by elongating the volume of one or both of the mixing area 112 and the vaporization chamber 216 in a vertical direction perpendicular to the plane of the showerhead 113, such that a pressure gradient is created in the vertical direction.
- Elongating one or both of the mixing area 212 and the vaporization chamber 216 may include elongating the respective volumes to have an aspect ratio between a length in the vertical direction and a width or diameter thereof that is greater than 2:1, 4:1, 6:1, 8:1, 10:1 or a value in a range defined by any of these values.
- one or both of the mixing area 212 the vaporization chamber 216 may include a continuously adjustable conductance-controlling means at lower portions thereof, such as a pressure regulator or a butterfly valve or the like, such that the local pressures therein are controlled to be higher than that of the gas pressure in the thin film deposition chamber 104 (FIG. 2).
- a continuously adjustable conductance-controlling means at lower portions thereof, such as a pressure regulator or a butterfly valve or the like, such that the local pressures therein are controlled to be higher than that of the gas pressure in the thin film deposition chamber 104 (FIG. 2).
- the downstream pressure control system 540 is configured to actively control the liquid precursor downstream of the liquid injection unit 112, e.g., in the mixing area 212 and/or the vaporization chamber 216, using the gas pressure sensing means 544 and the gas pressure control means 548.
- the gas pressure sensing means 544 and the gas pressure control means 548 may at least partly automatically or algorithmically regulate the downstream of the liquid injection unit 112, e.g., in the mixing area 212 and/or the vaporization chamber 216, in conjunction with the central control unit 550.
- the total pressure in the thin film deposition chamber 104 may be 0.001.0-3.0 Torr, 3.0-5.0 Torr, 5.0-7.0 Torr, 7.0-10.0 Torr, or a pressure in range defined by any of these values.
- the PPGI may be the same or different and be 0.001.0-3.0 Torr, 3.0- 5.0 Torr, 5.0-7.0 Torr, 7.0-10.0 Torr, or a pressure in range defined by any of these values.
- the local pressures in one or both of the mixing area 212 and the vaporization chamber 216 may be set or increased to be higher relative to the thin film deposition chamber 104, e.g., by more than 10%, 20%, 50%, 100%, 200%, 500%, or a percentage in a range defined by any of these values, e.g., 0.002.0-3.0 Torr, 3.0-5.0 Torr, 5.0-7.0 Torr, 7.0-9.0 Torr. 9.0-12 Torr, or a value in a range defined by any of these values.
- FIGS 6A-6C illustrate thin film deposition processes in which the liquid precursor delivery methods and systems according to embodiments can be implemented.
- Representative examples of thin film processes in which the liquid precursor delivery according to embodiments can be implemented include chemical vapor deposition (FIG. 6A), atomic vapor deposition (FIG. 6B) and atomic layer deposition (FIG. 6C).
- FIGS. 6A-6C is a schematic graph depicting a precursor parameter in the y-axis and time in the x- axis.
- the precursor parameter may include, e.g., a precursor flow rate, precursor partial pressure or a chamber pressure due to precursor introduction.
- FIGS. 6A-6C depicts a first precursor 610 and a second precursors 620.
- first and second precursors 610, 620 can be liquid precursor(s), or one but not the first and second precursors 610, 620 can be a liquid precursor.
- the first precursor 610 can be an oxidizing precursor, e.g., O2 or NH3, from the gas panel 116 (FIG. 2) and the second precursor can be liquid precursor 228 (FIG. 2), e.g., a metal precursor.
- One or both of the first and second precursors 610, 620 can be introduced with a carrier gas. While only two precursors are shown for illustrative purposes, it will be understood that there can be more than two precursors.
- FIG. 6A is a graph schematically illustrating precursor parameters as a function of time during deposition of a thin film using a continuous deposition process, e.g., chemical vapor deposition (CVD).
- the illustrated continuous deposition process comprises introducing the first precursor 610 and the second precursor 610 simultaneously or in a temporally overlapping manner into the thin film deposition chamber 104 (FIG. 2).
- FIG. 6C is a graph schematically illustrating precursor parameters as a function of time during deposition of a thin film using a cyclical deposition, e.g., atomic layer deposition (ALD).
- the illustrated cyclic deposition process comprises cyclically introducing a pulse of the first precursor 610, followed by a pulse of the second precursor 620.
- the exposure times or pulse times of each of the first and second precursors 610, 620 can be in the range of about 0.1-1 sec., 1-10 sec., 10-30 sec., 30-60 sec., or a duration in a range defined by any of these values.
- the cycle 310 may be repeated multiple times to deposit a desired thickness of the thin film.
- the pulses of the first precursor 610 and the pulse of the second precursor 620 may be accompanied or separated by a purge gas.
- the purge gas may be continuous or pulsed.
- Examples of purge a gas which may be used include, but are not limited to, helium (He), argon (Ar), nitrogen (N2), hydrogen (H2), and mixtures thereof.
- the cycles of the first and second precursors 610, 620 do not overlap in time. However, examples are not so limited, and there may be a partial overlap between the cycles.
- the pulses of the purge may be introduced into the thin film deposition chamber 104 (FIG. 2) continuously or as pulses separating by the pulses of the first and second precursors 610 and 620.
- pulses of the first precursor 610 and the second precursor 620 may be separated by pump evacuation, without a purge gas.
- FIG. 6B is a graph schematically illustrating precursor parameters as a function of time during deposition of a thin film using a hybrid deposition, e.g., atomic vapor deposition (AVD).
- the illustrated hybrid deposition process comprises cyclically introducing pulses of the second precursor 620 while introducing the first precursor 610 continuously or in pulses spanning at least one pulse of the second precursor 620.
- the exposure times or pulse times of the second precursor 620 and the first precursor 610 when pulsed can be in the range of about 0.1-1 sec., 1-10 sec., 10-30 sec., 30-60 sec., or a duration in a range defined by any of these values.
- the first precursor 610 spans a plurality of the pulses of the second precursor.
- the first precursor may span, partially or completely, only one pulse of the second precursor 620.
- One or both of the first precursor 610 and the second precursor 620 may be accompanied by a carrier or purge gas.
- the purge or carrier gas may be continuous or pulsed, and may include, but are not limited to, helium (He), argon (Ar), nitrogen (N2), hydrogen (H2), and mixtures thereof.
- the methods and systems for delivering a liquid precursor into a thin film deposition chamber can configured for a liquid precursor including B, N, Al, Si, P, Ti, V, Cr, Mn, Fe, Co, Ni, Zn, Ga, Ge, As, Se, Sr, Y, Zr, Nb, Mo, Ru, Ag, Cd, Sn, Sb, Ba, Hf, Ta, W, Re, Ti, La and Er, among others.
- Liquid precursors for a metal can be a metal halide or a metalorganic compound such as metal 0-diketonates, metal cyclopentadienyls, metal alkoxides, metal alkyls, and metal alkylamides, depending on the organic complex associated to the metal.
- the liquid precursor can a precursor in liquid state or a solid precursor dissolved in a solvent.
- the liquid precursors can be used to form metal oxides, metal nitrides, compound semiconductors, chalcogenides, fluorides and elemental metals, among other compounds.
- FIG. 7 illustrates an experimental graph of measured mass flow rate as a function of time for a liquid precursor introduced in pulse mode using a delivery method according to embodiments.
- the y-axis is the flow rate in standard cubic centimeters per minute (seem) and the x-axis represents time (hr: min: sec).
- the pulses of the liquid precursor has a duration of about 60 seconds.
- the mass flow rate is highly constant within pulse and reproducible pulse-to-pulse.
- the time duration for defining a manufacturing tolerance can be the duration of a single pulse, or an aggregate sum of a plurality of depositions.
- the time duration can exclude the initial spike when the liquid precursor delivery unit 112 (FIG. 2) is initially activated.
- the words “comprise,” “comprising,” “include,” “including” and the like are to be construed in an inclusive sense, as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including, but not limited to.”
- the word “coupled”, as generally used herein, refers to two or more elements that may be either directly connected, or connected by way of one or more intermediate elements.
- the word “connected”, as generally used herein, refers to two or more elements that may be either directly connected, or connected by way of one or more intermediate elements.
- conditional language used herein such as, among others, “can,” “could,” “might,” “may,” “e.g.,” “for example,” “such as” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or states.
- conditional language is not generally intended to imply that features, elements and/or states are in any way required for one or more embodiments or whether these features, elements and/or states are included or are to be performed in any particular embodiment.
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Abstract
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CN202180078061.8A CN116568860A (en) | 2020-11-19 | 2021-10-29 | Liquid precursor injection for thin film deposition |
EP21895847.8A EP4247507A1 (en) | 2020-11-19 | 2021-10-29 | Liquid precursor injection for thin film deposition |
JP2023528947A JP2023550356A (en) | 2020-11-19 | 2021-10-29 | Liquid precursor injection for thin film deposition |
KR1020237020121A KR20230129391A (en) | 2020-11-19 | 2021-10-29 | Liquid precursor spraying for thin film deposition |
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US16/952,493 US11459654B2 (en) | 2020-11-19 | 2020-11-19 | Liquid precursor injection for thin film deposition |
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Citations (4)
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US20040013800A1 (en) * | 2000-11-20 | 2004-01-22 | Strauch Gerhard Karl | Device and method for feeding a liquid starting material, which has been brought into the gaseous state, into a CVD reactor |
WO2012175334A2 (en) * | 2011-06-22 | 2012-12-27 | Aixtron Se | Method and device for depositing oleds, in particular evaporation device therefor |
US20170056912A1 (en) * | 2014-05-09 | 2017-03-02 | Korea Institute Of Industrial Technology | Liquid precursor delivery system |
US20180148836A1 (en) * | 2014-07-01 | 2018-05-31 | Aixtron Se | Apparatus and method for generating a vapor for a cvd or pvd device |
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AU9507298A (en) | 1997-09-26 | 1999-04-23 | Advanced Technology Materials, Inc. | Liquid reagent delivery system |
JP4393677B2 (en) * | 1999-09-14 | 2010-01-06 | 株式会社堀場エステック | Liquid material vaporization method and apparatus, and control valve |
US6548112B1 (en) * | 1999-11-18 | 2003-04-15 | Tokyo Electron Limited | Apparatus and method for delivery of precursor vapor from low vapor pressure liquid sources to a CVD chamber |
US7163197B2 (en) | 2000-09-26 | 2007-01-16 | Shimadzu Corporation | Liquid substance supply device for vaporizing system, vaporizer, and vaporization performance appraisal method |
DE10059386A1 (en) | 2000-11-30 | 2002-06-13 | Aixtron Ag | Method and device for the metered delivery of small liquid volume flows |
US20030019428A1 (en) * | 2001-04-28 | 2003-01-30 | Applied Materials, Inc. | Chemical vapor deposition chamber |
FR2874028B1 (en) * | 2004-08-06 | 2006-10-27 | Qualiflow Sa Sa | DEVICE FOR INTRODUCTION IN AN ENCLOSURE OF LIQUID PRECURSORS IN PULSE MODE WITH MEASUREMENT AND CONTROL OF THE FLOW |
FR2900070B1 (en) * | 2006-04-19 | 2008-07-11 | Kemstream Soc Par Actions Simp | DEVICE FOR INTRODUCING OR INJECTING OR SPRAYING A MIXTURE OF VECTOR GAS AND LIQUID COMPOUNDS AND METHOD FOR CARRYING OUT SAID DEVICE. |
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- 2021-10-29 CN CN202180078061.8A patent/CN116568860A/en active Pending
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US20040013800A1 (en) * | 2000-11-20 | 2004-01-22 | Strauch Gerhard Karl | Device and method for feeding a liquid starting material, which has been brought into the gaseous state, into a CVD reactor |
WO2012175334A2 (en) * | 2011-06-22 | 2012-12-27 | Aixtron Se | Method and device for depositing oleds, in particular evaporation device therefor |
US20170056912A1 (en) * | 2014-05-09 | 2017-03-02 | Korea Institute Of Industrial Technology | Liquid precursor delivery system |
US20180148836A1 (en) * | 2014-07-01 | 2018-05-31 | Aixtron Se | Apparatus and method for generating a vapor for a cvd or pvd device |
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US11459654B2 (en) | 2022-10-04 |
EP4247507A1 (en) | 2023-09-27 |
JP2023550356A (en) | 2023-12-01 |
CN116568860A (en) | 2023-08-08 |
KR20230129391A (en) | 2023-09-08 |
US20220154332A1 (en) | 2022-05-19 |
TW202227658A (en) | 2022-07-16 |
US20230128366A1 (en) | 2023-04-27 |
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